Package 62037-720-01

{"route": ["ORAL"], "spl_id": "01fbdb24-0987-40f6-a920-f36349f6ba61", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["db002ae3-f54c-40a4-9cb4-e5681bf426e3"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-720-01)", "package_ndc": "62037-720-01", "marketing_end_date": "20270430", "marketing_start_date": "20020410"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-720-05)", "package_ndc": "62037-720-05", "marketing_end_date": "20260630", "marketing_start_date": "20020410"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-720-10)", "package_ndc": "62037-720-10", "marketing_end_date": "20261231", "marketing_start_date": "20020410"}], "brand_name": "Potassium Chloride", "product_id": "62037-720_01fbdb24-0987-40f6-a920-f36349f6ba61", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "62037-720", "generic_name": "Potassium Chloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/1"}], "application_number": "ANDA075604", "marketing_category": "ANDA", "marketing_end_date": "20270430", "marketing_start_date": "20020410"}